Energy Charged Liquids to Enhance Enerceutical Activation of the Alternative Cellular Energy (ACE) Pathway in the Therapy of Diseases

ABSTRACT

The alternative cellular energy (ACE) pathway provides a non-immunological defense mechanism against infectious diseases and can also function as an effective, non-scarring, tissue repair mechanism in response to injury. The ACE pathway can be activated using energy obtained from the ultraviolet light illumination of neutral red dissolved in alcohol. The effectiveness of the alcohol used in this procedure is significantly increased by first bubbling air containing “Water Gas” (otherwise referred to as Brown&#39;s Gas or HHO) through the alcohol. The Water Gas is considered as providing an additional charge to the alcohol. Water Gas can similarly be used to charge water and other liquids and to, thereby, increase the liquid&#39;s capacity to interact with various dyes, such as neutral red, and with other enerceuticals, which are regarded as being representative of the body&#39;s ACE pigments. Various uses are disclosed for using Water Gas charged alcohol and Water Gas charged water, for the therapeutic activation of the ACE pathway.

CROSS REFERENCE TO RELATED APPLICATIONS

Co-Pending Patent Application

Methods for Detection of Ultraviolet Light Reactive Alternative Cellular Energy Pigments (ACE-pigments) William John Martin Submitted Dec. 24, 2007. Publication number 20090163831

Method of assessing and of activating the alternative cellular energy (ACE) pathway in the Therapy of Diseases. William John Martin Submitted Submitted Jan. 16, 2008. Publication number 20090181467

Enerceutical mediated activation of the alternative cellular energy (ACE) pathway in the therapy of diseases. Submitted May 8, 2008. Publication number 20090280193 Enerceutical activation of the alternative cellular energy (ACE) pathway in therapy of diseases. Submitted Feb. 11, 2009. Publication number 20090202442

Method of using the body's alternative cellular energy pigments (ACE-pigments) in the therapy of diseases Submitted Feb. 20, 2009. Publication number 20100215763 Urine as a source of alternative cellular energy pigments (ACE-pigments) in the assessment and therapy of diseases. Submitted Mar. 5, 2009. Publication number 20100196297

Diagnostic value of systemic ACE pathway activation in the detection by fluorescence of localized pathological lesions. Submitted Jul. 26, 2010. Publication number 20100291000

Enerceutical mediated activation of the alternative cellular energy (ACE) pathway in the therapy of diseases. Submitted July 2010.

Other Relevant Patents and Patent Applications by William John Martin:

Stealth viruses nucleic acids and related methods. U.S. Pat. No. 5,703,221. Issued Dec. 30, 1997.

Isolated stealth viruses and related vaccines. U.S. Pat. No. 5,753,488. Issued May 19, 1998.

Stealth virus detection in the chronic fatigue syndrome. U.S. Pat. No. 5,985,546. Issued May 26, 1998.

Stealth virus detection in the chronic fatigue syndrome. U.S. Pat. No. 5,985,546. Issued Nov. 16, 1999.

Method of generating hydrogen in gasoline using an enerceutical product added to magnesium in a hydrogen permeable but solute impermeable container. Submitted Jul. 18, 2008. Publication number 20100011657

Method of generating hydrogen and of selectively transferring the generated hydrogen to drinking water as a potential source of alternative cellular energy (ACE). Submitted Jul. 9, 2008. Publication number 20100008849

Method of generating hydrogen in drinking water using an enerceutical product added to magnesium in a hydrogen permeable but solute impermeable container. Submitted Jul. 14, 2008. Publication number 20100008850

Martin W J, Palmer S B. Regenerative wound healing using copper-silver citrate composition. Submitted Oct. 22, 2008. Publication number 20100099758 Apr. 22, 2010.

Patents and Patent Applications Relevant to the Present Application by Other Inventors: Water Gas (Also called Brown's Gas and HHO)

William Rhodes et al Apparatus for the electrolytic production of hydrogen and oxygen for the safe combustion thereof Patent number US003262872 Issued Jul. 26, 1966Horvath; Stephen. Fuel supply apparatus for internal combustion engines. U.S. Pat. No. 3,980,053. Issued Sep. 14, 1976.

Brown, Yull. Welding. U.S. Pat. No. 4,014,777 Issued Mar. 29, 1977.

Brown, Yull Arc-assisted oxy/hydrogen welding U.S. Pat. No. 4,081,656. Issued Mar. 28, 1978.

Inoue, Kiyoshi. Method of electrolytically generating hydrogen and oxygen for use in a torch or the like. U.S. Pat. No. 4,184,931 Issued Jan. 22, 1980.

McCambridge, Michael Electrolysis Of Water. U.S. Pat. No. 4,726,888 issued Feb. 23, 1988

Willey, Alan P. Radford, Neal T. Apparatus for gas generation. U.S. Pat. No. 5,082,544. Issued Jan. 21, 1992.

Chiang ,Huang C. Apparatus for generating a mixture of hydrogen and oxygen for producing a hot flame. U.S. Pat. No. 5,244,558 Issued Sep. 14, 1993. Oshima, Yujiro Hydrogen Generator. U.S. Pat. No. 5,401,371. Issued Mar. 29, 1995 Stowe, Gene B. Hydrogen/Oxygen Fuel Cell. U.S. Pat. No. 5,231,954 Issued Aug. 3, 1995.

Shiramizu, Yoshimi, Nakamori, Masaharu, Aoki, Hidemitsu, Seo, Hirofumi, Hamano;

Ross, Bill. Internal combustion engine kit with electrolysis cell. U.S. Pat. No. 6,209,493. Issued Apr. 3, 2001.

Klein; Dennis. Hydrogen generator for uses in a vehicle fuel system. U.S. Pat. No. 6,866,756. Issued Mar. 15, 2005.

Holt, Cecil G, Baker, Toby D, Speight, John Leland, Anderson Iboynne M, Salmon, Jeff, Stevens, David. Water fuel convertor. U.S. Pat. No. 7,261,062. Issued Aug. 28, 2007. Klein, Dennis J. Santilli, Ruggero Maria; Apparatus and method for the conversion of water into a new gaseous and combustible form and the combustible gas formed thereby. Patent application number 20040149591. Published Aug. 5, 2004.

Klein; Dennis. Apparatus and method for the conversion of water into a clean burning combustible gas for use as an additive with other forms of fuels. Patent application number 20070151846. Published Jul. 5, 2007.

Kang, Song Doug. Use of brown's gas and feeding apparatus of the brown's gas. Patent application number 20070104797. Published May 10, 2007.

Heath; Kevin; Gardner; Barry; Lang; Bill; Lang; Tom. System and method for improving fuel economy in combustion engines. Patent application number 20100147232. Published Jun. 17, 2010.

Kang, Song Doug. Method of treating or alleviating the symptoms of a lesion in mammal. Patent application number 20100173008 Published Jul. 8, 2010 Dees, James D, Colclesser, Ken. Hydrogen generator designed for use with gas and diesel engines. Patent application number 20100282600. Published Nov. 11, 2010. Haruto. Method for producing electrolyzed water U.S. Pat. No. 5,543,030 Issued Aug. 6, 1996.

Water Used as Therapy

Shimamune, Takayuki, Tanaka, Masashi, Nakajima, Yasuo, Nishiki, Yoshinori, Shimizu, Hideto. Production method of acid water and alkaline water. U.S. Pat. No. 6,527,940. Issued Mar. 4, 2003.

Norton, Verdis, Samuelson, Gary L. Method and apparatus for producing a stabilized antimicrobial non-toxic electrolyzed saline solution exhibiting potential as a therapeutic. Patent application number 20090110749. Published Apr. 30, 2009.

Chen, Ho-Hsien, Huang, Tzou-Chi, Huang, Hao-Hsun, Tung, Jung-Chang. Method for generating high concentration chlorine dioxide by means of electrolysis. Patent application number 20080308428. Published Dec. 18, 2008

Fukai, Toshiharu. Water Having Anticancer Activity and Method for Making the Same. Patent application number 20100233071. Publishe Sep. 16, 2010

Electrolyzer cell for producing acidic or alkaline water. Patent application number 20100270172. Published Oct. 28, 2010

Haase, Steven, Haase; Sherry, Holle, Greg, Holle, Tamera. Ionic foot bath array. Patent application number 20090069870. Published Mar. 12, 2009.

References to Published Articles Relevant to the Present Patent Application Alternative Cellular Energy Pigments (ACE-pigments):

-   -   1. Martin W J. Alternative cellular energy pigments mistaken for         parasitic skin infestations. Exp. Mol. Path 78: 212-214, 2005.     -   2. Martin W J. Alternative cellular energy pigments from         bacteria of stealth virus infected individuals. Exp. Mol. Path         78: 217-217, 2005.     -   3 Martin W J. Progressive Medicine. Exp Mol Path 78: 218-220,         2005.     -   4 Martin W J, Stoneburner J. Symptomatic relief of herpetic skin         lesions utilizing an energy based approach to healing. Exp. Mol.         Path 78: 131-4, 2005.     -   5 Martin W J. Etheric Biology. Exp Mol Path 78: 221-227, 2005.     -   6 Martin W J. Stealth Virus Culture Pigments: A Potential Source         of Cellular Energy. Exp. Mol. Pathol. 74: 210-223, 2003.     -   7 Martin W J. Complex intracellular inclusions in the brain of a         child with a stealth virus encephalopathy. Exp. Mol. Pathol. 74:         179-209, 2003.     -   8 Martin W J. Photons and phonons: Theoretical aspects of         biophysics and potential therapeutic applications. Proceeding of         Neural Therapy Workshop on Sound and Light Therapy, Seattle,         Wash., Feb. 21-23, 2003.

Stealth Adapted Viruses

-   -   1 Martin W J Chronic fatigue syndrome among physicians. A         potential result of occupational exposure to stealth viruses.         Explore 2001; 10: 7-10.     -   2 Martin W J. Stealth Viruses. Explore 2001; 10: 17-19.     -   3 Durie G M, Collins R. Martin W J. Positive stealth virus         cultures in multiple myeloma. A possible explanation for         neuropsychiatric co-morbidity. Presented at the Am. Soc.         Hematology annual meeting October 2000.     -   Martin W J. Chemokine receptor-related genetic sequences in an         African green monkey simian cytomegalovirus-derived stealth         virus. Exp Mol Pathol. 2000; 69:10-6.     -   5 Martin W J., Anderson D. Stealth virus epidemic in the Mohave         Valley: severe vacuolating encephalopathy in a child presenting         with a behavioral disorder. Exp Mol Pathol. 1999; 66:19-30.     -   6 Martin W J. Melanoma growth stimulatory activity         (MGSA/GRO-alpha) chemokine genes incorporated into an African         green monkey simian cytomegalovirus-derived stealth virus. Exp         Mol Pathol. 1999; 66:15-8.     -   7 Martin W J. Bacteria-related sequences in a simian         cytomegalovirus-derived stealth virus culture. Exp Mol Pathol.         1999; 66:8-14.     -   8 Martin W J. Stealth adaptation of an African green monkey         simian cytomegalovirus. Exp Mol Pathol. 1999; 66:3-7.     -   9 Martin W J. Cellular sequences in stealth viruses.         Pathobiology 1998; 66:53-8.     -   10 Martin WJ. Detection of RNA sequences in cultures of a         stealth virus isolated from the cerebrospinal fluid of a health         care worker with chronic fatigue syndrome. Case report.         Pathobiology. 1997; 65:57-60.     -   11 Martin W J., Anderson D. Stealth virus epidemic in the Mohave         Valley. I. Initial report of virus isolation. Pathobiology.         1997; 65:51-6.     -   12 Martin W J. Simian cytomegalovirus-related stealth virus         isolated from the cerebrospinal fluid of a patient with bipolar         psychosis and acute encephalopathy. Pathobiology. 1996; 64:64-6.     -   13 Martin WJ. Stealth viral encephalopathy: report of a fatal         case complicated by cerebral vasculitis. Pathobiology. 1996;         64:59-63.     -   14 Martin W J. Genetic instability and fragmentation of a         stealth viral genome. Pathobiology. 1996; 64:9-17.     -   15 Martin W J. Severe stealth virus encephalopathy following         chronic-fatigue-syndrome-like illness: clinical and         histopathological features. Pathobiology. 1996; 64:1-8.     -   16 Martin W J. Stealth virus isolated from an autistic child. J         Autism Dev Disord. 1995; 25 :223-4.     -   17 Gollard R P, Mayr A., Rice D A, Martin W J.         Herpesvirus-related sequences in salivary gland tumors. J Exp         Clin Cancer Res., 1996; 15: 1-4.     -   18 Martin W J., Glass R T. Acute encephalopathy induced in cats         with a stealth virus isolated from a patient with chronic         fatigue syndrome. Pathobiology. 1995; 63:115-8.     -   19 Martin W J, et al. African green monkey origin of the         atypical cytopathic ‘stealth virus’ isolated from a patient with         chronic fatigue syndrome. Clin Diag Virol 1995: 4: 93-103.     -   20 Martin W J. Stealth viruses as neuropathogens. CAP Today.         1994; 8: 67-70.     -   21 Martin W J. et al. Cytomegalovirus-related sequence in an         atypical cytopathic virus repeatedly isolated from a patient         with chronic fatigue syndrome. Am J Pathol. 1994; 145: 440-51.

Discovery of Low Density/High Energy Water and High Density/Low Energy Water

Wiggins P M. High and low density water in gels. Prog Polymer Sci. 1995; 20:1121.

Wiggins P. High and low density water and resting, active and transformed cells. Cell Biol Internat. 1996; 20:429-435.

Wiggins P. Life depends upon two kinds of water PLoS 2008; 3:e1406.

Wiggins P. High and low density intracellular water. Cell Mol Biol. 2001 Jul;47:735-44.

Potential Biosynthetic Capacity of Alcohol

Watson A J, Williams J M. Chemistry. The give and take of alcohol activation. Science. 2010; 329: 635-6.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not applicable: No Federal funding was received in support of this patent application.

REFERENCE TO SEQUENCE LISTING, A TABLE OR A COMPUTER PROGRAM LISTING COMPACT DISK APPENDIX

Not applicable.

BACKGROUND OF THE INVENTION:

The invention is based on the following broad conceptual understanding on how the body can acquire cellular energy other than through the oxidative metabolism of foods. Essentially, an alternative cellular energy (ACE) pathway has been identified that is mediated by the direct energy converting (transducing) properties of various materials, arbitrarily termed alternative cellular energy pigments (ACE pigments). Cellular energy generated by this pathway complements the chemical energy, which is derived by living organisms from the metabolism of food. The ACE pathway is postulated to contribute to various physiological functions of the body. Of particular relevance to this application, the ACE pathway is involved in non-inflammatory defense and tissue repair mechanisms. An inadequacy of the ACE pathway can render an individual susceptible to infection, especially if their immune system is impaired or if they become infected with microbes, which cannot evoke a cellular immune response. An inadequate ACE pathway can also limit the body's capacity to recover from traumatic injuries; resulting in delayed wound healing with excessive scarring from over reliance on trauma evoked inflammatory reactions. The ACE pathway is also anticipated to be involved in the normal functioning of many organs, including the brain. Moreover, it is reasonable to presume that many illnesses, not necessarily of infectious origin, may place an added burden on the ACE pathway, causing an inadequacy or deprivation of the ACE pathway with a resulting delaying of the natural healing process. Conversely, augmenting or correcting an impaired ACE pathway may facilitate recovery from a wide range of various illnesses. Moreover, a fully functioning ACE pathway is likely to be a factor in maintaining wellness, enhancing athletic performance, increasing cognitive abilities, etc.

The body's ACE pigments are envisioned as tiny batteries with differing levels of being “charged.” The working model postulates that uncharged or very poorly charged ACE pigments will not fluoresce when illuminated directly with an ultraviolet light, (for example a 13 watt Halco spiral UV light bulb or a Streamlight 365 nm LED stylus penlight.) They will, however, fluoresce when mixed with certain dyes, including neutral red (e.g. at 0.1 mg/ml; available from Dudley Chemicals, New Jersey). ACE pigments can also alter the fluorescence pattern of other dyes, including acridine orange and Stains-All. Once partially charged, certain ACE pigments will fluoresce directly when illuminated with UV light. The UV illumination is able to provide additional energy to the ACE pigments, such that when more fully charged, the ACE pigments will no longer fluoresce under UV illumination in either the presence or absence of neutral red dye. The three energy levels classification of ACE pigments has proven useful in the clinical assessment of patients.

Particles of ACE pigments can be collected from areas of skin and skin lesions, hair, body fluids, including perspiration, saliva, urine and blood. In blood, the ACE pigments can be seen both within cells, including neutrophils and can also be detected as microscopic particles in serum/plasma samples. A simple home based fluorescence screening method is for people to collect saliva, perspiration and/or urine onto a suitable gauze swab, sponge, wooden spatula, cotton Q-tip and certain filter papers and to test for UV fluorescence, before and particularly after the addition of neutral red dye. Direct fluorescence of the body's ACE pigments can also be tested by directly shining a UV light onto the skin, or preferably within the mouth. This testing is based on the indication that partially charged ACE pigments are expected to directly fluoresce with UV illumination.

As disclosed in prior patent application, ACE pathway activation has provided a therapeutic measure for use in patients with a wide range of illnesses. It is possible, for example, to utilize ACE pigments in the therapy of herpes simplex virus (HSV) induced skin lesions. ACE pigments can be collected directly from the skin lesion or, if present, from bodily fluids, including perspiration, saliva and even urine. The collected material is reacted with a solution of freshly prepared neutral red dye, which is placed onto the HSV skin lesion and illuminated with a UV light. A healing energy is transferred to the underlying HSV skin lesion, as shown by the lesion becoming fluorescent when directly illuminated with the UV light. The fluorescence typically takes 1-2 minutes to begin and persists for several minutes before beginning to fade. Patients experience symptomatic relief from acute symptoms and the lesions show marked expedited healing over the ensuring 24-48 hours.

Major developments in this procedure have included the following: i) Direct contact of the neutral red dye solution with the underlying HSV skin lesion is not required. Thus, the collected ACE pigments with neutral red dye solution can be placed onto a water impermeable surgical towel or placed within a plastic bag, (e.g. Zoploc bag), which is then laid onto a water moistened HSV skin lesion. ii) The procedure can be adapted to treat areas of the skin on which prior outbreaks of HSV skin lesions have occurred and future outbreaks might otherwise be expected. Perspiration collected from these areas of skin will commonly show the presence of “uncharged” ACE pigments, meaning that they will fluoresce when mixed with freshly prepared neutral red solution. This material, as well as other neutral red inducible fluorescing bodily fluids, such as saliva, can be used to activate direct UV skin fluorescence in the areas on which HSV recurrences might otherwise occur. By doing so, the likelihood of any further recurrences, even in emotionally stressful situations, has been markedly reduced. iii) The need for collecting ACE pigments from the patients has been eliminated by the development of various solutions which can directly, or indirectly, lead to the fluorescing of ACE pigments. Early solutions included a 10% alcohol (ethanol) solution with trace quantities of herbal products plus 1% Lidocaine. This formulation fluoresced brightly with the addition of neutral red and UV illumination. Moreover, microscopically visible, un-dissolved neutral red particles displayed persisting and vigorous movements within the herbal solution. Certain other products, such as a fluorescing oil from the leaves and seeds of moringa trees, would directly fluoresce under UV illumination and transfer a fluorescing capacity to uncharged ACE pigments within virus induced skin lesions. A terpene-rich tree sap product produced in Japan and marketed as EH-101 and HB-101, was also effective, especially when mixed with alcohol. It was next discovered that neutral red dye would fluoresce with dissolved directly into alcohol, and that this mixture was as effective as the Lidocaine containing herbal formulation in activating patient's ACE pigments.

The focus of therapy was also switched from treating patients with conventional herpes and papillomavirus infections, including HSV, herpes zoster virus (HZV) shingles and post-herpetic neuralgia, and genital warts caused by HPV; and towards the goal of treating children with autism and adults with mental illnesses. Prior research had indicated a role for atypical viruses, which are unable to activate the cellular immune system, in the cause of autism and other illnesses with a significant impairment of normal brain functioning. The viruses were grouped under the term “stealth adapted viruses,” and many patients with autism, chronic fatigue syndrome (CFS) and major psychiatric illnesses are stealth adapted virus infected, as shown by a virus culture method, which I developed.

In a similar sequence of studies as conduced on patients with HSV infections, I was able to show effective activation of the ACE pathway using i) perspiration, saliva and even urine derived ACE pigments from an autistic child to which freshly prepared neutral red dye was added, and sprayed onto either water impermeable surgical towels or placed within a Ziploc plastic bag, placed onto the broad areas of the skin of the child and illuminated with UV light. ii) The Lidocaine plus herbal formulation containing 10% alcohol, used as an alternative to having to collect ACE pigments from the patient, in the aforementioned procedure. This approach initially provided far more convenience than parents having to collect ACE pigments from the child's bodily fluids. A problem arose in the clinical studies, however, when the Lidocaine plus herbal formulation lost its prior ACE pathway activating ability. I had no readily available explanation for the loss of activity.

The clinical ineffectiveness of the “expired” Lidocaine plus herbal formulation in systemically activating the ACE pathway in autistic children was supported by parents' failure to observe the development of direct fluorescence within the oral cavity of their child following the procedure. The development of new oral fluorescence or increased intensity of prior oral fluorescence had been a reliable indication of ACE pathway activation and correlated with apparent behavioral improvements. Other parents had associated clinically successful therapy with the development of discernable skin fluorescence not only beneath the treated skin area, e.g., the back or abdomen, but also on the feet, especially the soles. This observation had led to the choice of placing the Ziploc bags containing the activating solutions onto water-moistened soles of the feet of autistic children.

A temporary switch in treating children with autism was made from the ineffective Lidocaine plus herbal formulation to using moringa leaf and seed oil. I soon realized, however, that the Lidocaine plus herbal solution could be replaced by simply using absolute alcohol (200 proof ethanol). I further realized that the absolute alcohol solution with added neutral red could be stored for several days within a refrigerator and still prove effective in provoking direct UV fluorescence of the oral cavity. Clinical progress of a test subject has been quite remarkable over the last year with marked amelioration of her symptoms of autism. Therapy sessions have generally been administered at 3-4 week intervals, as monitored by emotional behaviors (self-awareness, memory of prior social encounters and empathy, expressed as a sense of humor) and by the desired minimizing of neutral red dye evoked fluorescence of the child's saliva. This patent application describes a further improvement in this basic procedure. To better understand this advance, it is appropriate to describe some additional background information, which might at first sight be considered unrelated to the ACE pathway.

In what began as an unrelated series of experiments, I have been producing a copper citrate solution, with and without silver, as an anti-bacterial product with particular efficacy against Gram positive bacteria, including methicillin resistant Staphylococcus aureus (MRSA). A Sears Diehard 12 Volt battery charger provides the electrical energy for electrolysis. Copper (and silver) anodes and a copper cathode are placed into a citric acid:potassium carbonate solution. A surprising and unexpected observation was the unmistakable, approximately 2-3% increase in the solution volume occurring during the 1-2 hours electrolysis. The expanded water volume persisted beyond the electrolysis process. Moreover, solutions stored for over a month would show a slight reduction in volume. The increased volume could be restored by 1-2 minutes of recharging with a 12 Volt battery. In addition to possessing anti-bacterial activity, the solution was reported by several patients as providing a very remarkable wound healing benefits. Although, initially painful when placed on an open wound, subsequent applications of the solution are well tolerated with far less pain. The expedited healing was also associated with far less scarring than would otherwise have occurred.

The observation of a volume increase in the solution was reminiscent of studies reported by Dr. Philippa Wiggins of New Zealand that water can exist as a mixture of low density, highly energized domains and high density, lower energy domains. She had suggested that individual water molecules expand by absorbing chemical energy, for example, derived from the conversion of ATP to ADP. The expanded water molecules return to the denser, smaller size as the energy is withdrawn to enable other chemicals to interact.

I had been interested in her study because I had previously noted that there was a fluid volume expansion during the formulation of Lidocaine plus herbal formulation, plus an apparent tendency for water to separate from the alcohol solution. Specifically, I would dissolve the Lidocaine in alcohol and gradually add water and/or water with diluted tinctures of various herbal components. By either adding water or allowing much of the alcohol to evaporate, the Lidocaine would come out of solution as fine long needles and/or non-structured flocculants. More interestingly, a clear separation would occur between a water layer below and an alcohol layer above a band containing the Lidocaine. Microscopically, the Lidocaine particles would show a flurry of kinetic movements with the formation of numerous gas bubbles. The total volume of the solution would also be slightly increased. By simply adding more alcohol to dissolve the Lidocaine, and then allowing the alcohol to partially evaporate, the precipitation and gas formation processes were repeatable over several cycles.

A possibly related observation is that a tincture of iodine (containing alcohol) added to an aqueous solution of Lidocaine, placed into the well of a culture dish, will stimulate a vigorous flurry of iodine containing droplets. The droplets settle to the surface of the dish with larger droplets gradually leading to the dissolving of smaller droplets in close proximity, but not actual contact with the larger droplets. Again, there is a separation with the iodine containing droplets being in an aqueous layer, which becomes separated from an overlaying alcohol layer.

Again, in a seemingly at first unrelated line of research, I became interested in augmenting the ignition quality of gasoline. I could produce hydrogen gas in gasoline by using magnesium metal in a magnesium chloride solution. I devised a hydrogen gas permeable membrane container into which I would place the metal and magnesium chloride. The membrane would allow the generated hydrogen, but not the magnesium or chloride ions, to mix with the gasoline. As an offshoot of these studies, I recalled earlier reports that it was possible to generate a novel form of ignitable water gas using electrolysis. This gas, which developed midway between the electrodes, was apparently different from steam and probably also different from a simple mixture of electrolysis generated hydrogen and oxygen gas. The basic observation of an ignitable water gas dates to the 19^(th) century, but was first patented as a potential gas for welding by William Rhodes in 1966. Mr. Yull Brown subsequently reported additional observations on the gas and also patented some of its potential industrial uses. The gas became more widely known as Brown's Gas or Brown Gas and offered as a possible replacement of acetylene in major industrial welding. In his patents, Mr. Yull Brown hypothesized that electrically separated “atomic” forms of oxygen and hydrogen were able to yield energy “in a number of complex chemical reactions.” I have found no evidence for this assumption and have, therefore, opted to use the term “Water Gas” rather than Brown's Gas in reference to my own studies on the gas arising, from what I believe is low density, high energy water molecules.

Several investigators suggested the potential use of what they call Brown's Gas, sometimes also referred to as HHO, to provide additional ignition energy for automobiles. Again, in most of these reports, the investigators have not clearly distinguished whether the gas being generated is hydrogen, a mixture of ordinary hydrogen and oxygen, atomic forms of separated hydrogen and oxygen, or, as I believe, an atypical form of water vapor. In virtually all cases, the gas is intended to be added to the air intake into the combustion chambers of the car and to essentially be an additive to the combustion energy provided from the ignition of gasoline.

I had earlier become aware of naturopathic practitioners wanting to have their patients consume the water condensing from an ignited “Brown Gas” welding flame. Supposedly, the water had some health benefits. Moreover, even though it is potentially flammable, I read an interesting patent by Dr. S. D. Kang on possible health benefits of spraying “Brown Gas” from a welding machine onto disease-affected areas of the body. He suggested that the gas was able to function as if it were water and to, thereby, carrying the equivalent of moisture into tissues. Dr. Kang also suggested the possibility of free hydrogen in the gas having potent anti-oxidizing activity in inhibiting inflammation. From Dr. Wiggins work, I reasoned that low density, high energy water was likely to be the source of the therapeutically useful gas. Arguably, it would have lost some of its energy in the vaporization process, but might still be able to add sufficient energy to existing high density, low energy water, leading to the water becoming more of the low density, high energy form. I further reasoned that if the electrolytically generated Water Gas could potentially add energy to regular water, might it not also be able to add energy to other liquids, and in particular, to alcohol? I chose this approach, since I knew that alcohol is non-conductive to electricity and I was reluctant to add electrolytes to alcohol in an electrolysis reaction, lest the alcohol might ignite.

Returning to the therapeutic uses of UV illuminated neutral red dissolved in alcohol and/or in Lidocaine plus herbal formulation, I, therefore, experimented on the possible additional benefits, which might be achieved by using a Water Gas activated alcohol and/or herbal solutions. I re-experimented with the copper citrate electrolysis and took note of the formation of gas bubbles, not only on the electrodes, but also from water well away from the electrodes. These non-electrodes associated bubbles were presumptively being formed by the vaporization of electrlytically generated low density, high energy water. I decided to devise ways of capturing this Water Gas use and to see if it would increase the reactivity of alcohol with neutral red and further enhance the therapeutic usefulness of the resulting solution. This patent application describes the utility of this approach and extends the basic finding to being able to add energy, subsequently referred to as charge) to other liquids.

BRIEF SUMMARY OF THE INVENTION

The passage of electrolytically derived Water Gas into alcohol greatly enhances the ability of the alcohol to react with neutral red dye and with the ACE pigments, such that when the mixtures are illuminated with visible and/or UV light, they can provide more ACE to an energy deficient individual, when compared with using untreated alcohol. Water Gas infused (charged) Lidocaine plus herbal formulations, as well as charged water and other liquids, are similarly more effective in their interaction with neutral red dye and with ACE pigments, than are the untreated (non-charged) control liquids. Methods are described for producing, monitoring and therapeutically using the charged liquids. Combining charged alcohol and charged water in various combinations or each alone, provides a range of solutions for various therapeutic applications. The applications include procedures, which do not require the direct contact of the charged solutions with the skin and/or mucus membranes. The charged solutions can also potentially be used for direct topical application to the skin and for parental injections, with or without the inclusion of neutral red dye and/or ACE pigments. The purpose of the invention is to simplify and to render more effective some of the existing therapeutic approaches aimed at enhancing the ACE pathway in humans and animals. The newly described methods are also applicable to the production of solutions useful in the assessment of the ACE pathway in an individual.

BRIEF DESCRIPTION OF THE DRAWINGS

Not Applicable and none included

DETAILED DESCRIPTION OF THE INVENTION

Until this invention, UV light illuminated neutral red dissolved in regular absolute alcohol (200 proof ethanol) has been the preferred method of choice for activating the ACE pathway in an individual. Approximately 5 mg of neutral red freshly dissolved in 10 ml of alcohol has generally been placed in a re-sealable plastic bag (Ziploc) with a small sheet of absorbent paper to help evenly distribute the fluid. The plastic bag is placed onto a moistened surface of the body to help minimize intervening air pockets, with taping as necessary. Preferred sites for placing the bags are the soles of the feet, palms of the hand and the face. The bag is usually illuminated with a 13 Watt spiral ultraviolet light bulb (Halco) positioned closely to the solution. In some experiments two 40 watts, 4 feet long tubular UV bulbs have been used. The illuminated solution shows a yellow-orange fluorescence in a darkened room. The therapy session will typically last from 30-60 minutes. Before, during and after the procedure, the treated area and the oral cavity are examined for using the same type of Halco UV light, or a more focused UV Streamlight 365 nm LED penlight. In an ACE deficient individual, one would expect to see the development of oral fluorescence as an indication of systemic activation of the ACE pathway. If no inducible fluorescence occurs within the oral cavity or elsewhere on the body, a tentative conclusion can be that there is unlikely to be a deficiency of the ACE pathway, which is correctable using this procedure.

I produced Water Gas by electrolysis of a 5 liter solution of citric acid and potassium carbonate (30 grams of each/1 with pH adjusted to 5.5). A plastic inverted funnel 4″ wide with attached flexible tubing was held just slightly above the surface of the solution. The funnel was placed between and away from the two electrodes, so as to minimize the collection of the hydrogen and oxygen gases coming directly from the electrodes. The other end of the flexible tubing from the funnel was attached to a 240 ml suction canister containing 200 ml alcohol with the inlet tube being inserted well down below the surface of the alcohol. The outlet tube from the suction canister was connected to a vacuum pump. The vacuum driven system was effective in bringing any Water Gas released from the electrolysis reaction, along with normal air entering from the sides of the collecting funnel, into the alcohol solution. Electrolysis and gentle vacuum suctioning proceeded for at least 4 hours. The Water Gas treated alcohol, from which some evaporation had occurred, was then compared with untreated alcohol in various assays.

The first test was to compare Water Gas treated versus control alcohol for its reactivity with very small quantities of neutral red powder. Pumping of the Water Gas through the alcohol solution clearly altered and enhanced its capacity to dynamically interact with the neutral red dye. Among the microscopic changes seen were more rapid dissolving of most of the neutral red particles, with more sharply defined and strikingly long narrow streams of dye coming from individual particles. Remaining small undissolved neutral red particles displayed pronounced and persisting back and forth movements, which were more marked than had been previously seen with regular alcohol. Microscopically one could easily observe individual particles moving towards each other to form a small clump of particles, but then to abruptly reverse direction and re-separate, only to again be re-attracted to each other and reform into a clump. Some particles stayed within the clumps while others displayed the back and forth movements. Similar, but less pronounced, movements are also observable when neutral red is added to untreated alcohol. No such movements are seen when neutral red is added to plain water.

The intensity of the attraction of particles into groups, followed by abrupt repulsion of particles from the groups, as seen with the treated and apparently “charged” alcohol was reminiscent of what I had previously observed, but never actually published on, with ACE pigment particles accumulating in long-term cultures of stealth adapted viruses. I had also previously noted that the addition of hydrochloric acid (HCl) would activate movements of the ACE pigment particles. This experiment was performed because of reports in the 1930's that intravenous HCl promoted the recovery from various illnesses. There was also an apparent reduction in needed oxygen in patients to whom HCl was injected. I inferred this from the published description of brighter red color of the treated patients' venous blood

An important and easily noticeable difference between the Water Gas treated and untreated alcohol—neutral red solutions is the more intense fluorescence of the solution containing Water Gas charged alcohol. It was clear that the Water Gas charged alcohol was more reactive than untreated alcohol. A determination of volume expansion could not be made because of evaporation, which occurred due to the bubbling of the Water Gas through the alcohol.

The working model is that neutral red dissolved in alcohol can respond to UV illumination by emitting a form of biological energy, which can travel beyond the actual neutral red in alcohol solution. The emitted biological energy can influence the motility pattern of unicellular microorganisms. This can be observed microscopically, if a droplet containing motile microorganisms is placed close to, but physically separated from the alcohol neutral red solution. For instance, a droplet containing visible, motile microorganisms is placed on top of a closed transparent Petri-like dish containing white plus UV light illuminated neutral red:alcohol solution. In a positive test, the microscopically visible microbes begin to display erratic, seemingly purposeless movements. While the effect was clearly seen with neutral red dissolved in regular alcohol, it was strikingly more apparent in the charged alcohol. Moreover, it became clear that even regular light from the microscope was quite effective in generating the distant effect, which UV illuminated alcohol:neutral red solutions can have on the motility of microbes. Indications of an effect of white light had earlier been noted with neutral red in regular alcohol, but were clearly more readily observed using the charged alcohol.

A similar series of experiments with confirmatory results was performed using a small, internet-available, Brown's Gas, or what I am prefering to call “Water Gas” generator (watertogas.com). The device, similar to that described in Patent Application 2010/0147232 “System and Method for Improving Fuel Economy in Combustion Engines,” was obtained from Mr. Bill Lang, one of the authors on the patent application. The basic unit is a 500 ml water bottle with electrodes extending down from two insulated holes placed into the lid. Sodium bicarbonate (1 teaspoon or approximately 3.5 gm) is added to approximately 350 ml of tap water to render it electrically conductive. Connecting the leads from a 4.5 DC 300 mA transformer to the electrodes produces electrolysis and gas formation in this “electrolyzer unit.” The stem of a “T” shaped tubing connection piece passes through the lid of the electrolyzer unit. One side of the “T” is connected to tubing coming from a small aquarium air pump. The other side of the “T” connects to tubing, which I extended below the surface of 100 ml alcohol solution placed in a nearby container. Air passing through the tubing over the electrolyzer unit is intended to collect the hydrogen, oxygen and Water Gas coming from the unit and carry it to the alcohol solution. I generally conducted the early experiments over 3-4 hours, with a loose lid placed over the alcohol container to help reduce evaporation of the alcohol. In more recent experiments, I switched from using sodium bicarbonate in tap water to 50% seawater, which generated more gas and reduced the time needed to showing a charging effect on the alcohol to less than 60 minutes.

I also developed a more standardized assay system for describing the interaction of neutral red particles placed into a liquid. Typically, only a few (usually less than 10) fine particles of neutral red powder, are added to the liquid in a small (1.5 sq inch) rectangular plastic dish. The particles are viewed microscopically as they begin to dissolve. A clear determination can be made of inactive (non-charged) liquids, such as regular water, in which slowly enlarging rings of defusing neutral red extend evenly around stationary neutral red particles. Neutral red particles display a far more dynamic response when placed into a regular alcohol solution. Narrow, single stream of soluble neutral red dye will typically emerge from individual particles. The dissolving particles, as well as small un-dissolved particles, will also be seen periodically, rapidly moving through the solution and occasionally interacting by either attraction or repulsion with other particles. By contrast, in Water Gas charged alcohol, much longer and narrower streams of dissolving neutral red dye come out more quickly from the dissolving particles. More impressive, are the speeds of the movements and the seeming strength of the attraction and repulsion forces, which especially affect the particles, which do not fully dissolve in the alcohol solution. These movements cease when the dish is removed from a light source, but rapidly resume when the dish is re-illuminated with light.

A person accustomed to testing his saliva for neutral red stainable ACE pigment particles reported that energetically moving microscopic particles were clearly more apparent when he added his saliva to the charged alcohol, than to regular alcohol. He confirmed that UV illuminated of a Ziploc bag containing neutral red dissolved in the charged alcohol, which he placed over the palms of his hands, was highly effective in systemically activating his ACE pathway, as evidence by enhancement of the direct UV fluorescence within his mouth, occurring shortly after beginning a treatment session. More importantly, he repeatedly used the charged alcohol: neutral red solution for over a month, without any apparent loss of its beneficial ACE pathway activation activity.

It is not unreasonable to suppose that the charged alcohol is able to continually absorb energy from the surroundings. Indeed, some of the absorbed energies would appear to be involved in possible lipid biosynthesis. This provocative suggestion arose from observing the formation of numerous small oily bubbles in long-term (1-2 months) stored charged alcohol:neutral red solutions. Aliquots from these stored solutions were placed into an open dish and observed microscopically for dynamically moving, still undissolved particles. Such particles were readily seen and their movements were clearly stimulated by both regular white light and UV light. More fascinating was the extensive formation of minute oily bubbles, which subsequently coalesced as the alcohol continued to evaporate. The oily bubbles did not incorporate the neutral red dye and were easily distinguishable from the neutral red colored alcohol. Some other materials, which were stained with neutral red, also precipitated out of the solution in very distinctive banding patterns. The potential of alcohol to engage in biosynthetic reactions, including the formation of carbon to carbon bonding, was recently mentioned in a Science publication.

The next extrapolation was that the wound healing benefits observed with the copper citrate solution might have been due, at least in part, to electrolysis energy activation of the water. I am well aware of the many claims made regarding ingesting water, which has been produced by electrolytic treatment of tap water. Typically, the water is separated on the basis of preferred ingestion of water with an alkaline pH and/or active electron donating activity (negative Oxidation-Reduction Potential, ORP). Other health practitioners have advocated electromagnetic radiation energies, magnetic energy and sound energies to enhance the health benefits of water. I was encouraged by Mr. Lang suggestion that drinking water into which he had passed some Brown's Gas, might have health benefiting effects and also on Dr. Kang's prior patent application of blowing what he was calling Brown's Gas onto a site of injury.

I, therefore, repeated the above experiments using the newly installed device to charge water rather than alcohol. Water into which the aquarium pump was delivering a stream of air, plus hydrogen, oxygen and Water Gas was periodically sampled and used to dissolve minute amounts of neutral red powder. The resulting solutions were also examined for possible UV fluorescence and for movement patterns of any un-dissolved fine particles of neutral red. While no fluorescence was seen in any of the resulting neutral red solutions, there were minor indications for enhanced movements and dynamic interactions among some of the un-dissolved neutral red particles.

The decision was next made to combine the Water Gas treated alcohol with the Water Gas treated water and to compare these solutions with those in which only one component had been charged. In terms of the intensity of fluorescence, and the light stimulated movements of un-dissolved neutral red particles, more of the activity seen with 100% charged alcohol was retained using lower alcohol concentrations diluted in charged water, when compared to the charged alcohol being diluted in uncharged water. Conversely, charged water was able to sustain the activity of diluted uncharged alcohol better than could uncharged water. A striking observation was the occasional cloudiness, which would immediately develop in the mixed charged water:charged alcohol solutions, seemingly because of the formation of very stable emulsion-like alcohol-water interactions.

Although not wanting to drink any of the charged water:charged alcohol-solutions, I did repeatedly and liberally apply both clear and cloudy solutions on my skin. I had previously heard from others that the copper citrate solution was helping with their skin complexion and had begun to see if I could confirm this effect. I soon realized there was a greater skin appearance enhancing activity present in the combined charged water: charged alcohol solutions. A beneficial effect was retained with as low as 5% alcohol.

Next, I proceeded to show that Lidocaine plus herbal formulations in 5-10% alcohol solutions could be enhanced in the intensity of fluorescence and in particle movements when used to dissolve neutral red if they were prepared with treated alcohol and treated water than when prepared in the usual manner using uncharged water and uncharged alcohol. As an alternative approach, electrolytically generated Water Gas was bubbled through a regularly prepared Lidocaine plus herbal formulation. This procedure was effective in enhancing the UV fluorescence and in stimulating the un-dissolved neutral red particle movement generating activity of the solutions. Lidociane will react with tincture of iodine to yield a flurry of rapidly moving iodine-containing droplets. This activity was enhanced using the charged Lidocaine plus herbal formulations. As part of these endeavors, I observed that tincture of iodine would actually form small droplets when placed directly into the charged alcohol. Thus, rather than being completely miscible, as it is with regular alcohol, some of the iodine separated into small droplets.

Finally, I have used electroylsis system used to bubble Water Gas through other solutions, some of which I have been studying for potential therapeutic purposes, including moringa leaf and seed oil, humic and fulvic acids, a terpene-rich tree sap solution called EH-101, a mineral-rich solution obtained by depleting sodium chloride by evaporation of water obtained from the Great Salt Lake and water to which I have added magnesium chloride. In each case, I have been able to document changes in reactivity of the liquid resulting from several hours of exposure to the electrolysis-generated Water Gas. I next tested a range of alcoholic beverages, including vodka, gin, whisky, brandy and wine, to see whether bubbling Water Gas through the liquids would affect their reactivity with added neutral red particles. While some indications of a positive effect has been seen, this approach is somewhat limited by the resulting reduction in the relative amount of alcohol content because of its greater tendency to evaporate compared to water.

In doing these studies, a few (usually less than 20) fine particles of neutral red powder, are added to the liquid in a small (1.5 sq inch) rectangular plastic dish. The particles are viewed microscopically as they begin to dissolve. A clear determination can be made of inactive (non-charged) liquids, such as regular water, in which slowly enlarging rings of defusing neutral red extend around stationary neutral red particles. Neutral red particles display a far more dynamic response when placed into a regular alcohol solution. Narrow, single stream of soluble neutral red dye will typically emerge from individual particles, added to by the movement of the particles. The dissolving particles, as well as small un-dissolved particles, will also be seen periodically, be much more rapidly moving through the solution and occasionally interacting, by either attraction or repulsion, with other particles. The long narrow streams of dissolving neutral red and both the speed of movement and the extent of particle to particle interaction are much more marked in Water Gas charged liquids, when compared with the same type of liquid, which has not been charged. With water, the effect is qualitative since there is essentially no particle movements in uncharged water, but clearly discernable activity in charged water. With alcohol, the effect is more quantitative with far greater activity being seen with charged versus uncharged alcohol. Combinations of charged water and charged alcohol are also far more active than using comparable combinations of uncharged water and uncharged alcohol.

This research has helped stimulate a new understanding of the ACE pathway, with many potential improvements on existing therapeutic efforts to enhance this pathway in the treatment of illnesses in humans and animals. If I assume that neutral red dye (and probably many herbal formulations) are comparable to forms of ACE pigments, then it seems that charging of alcohol and to a lesser extent the charging of water, facilitate the energy transfer to ACE pigments. Absorption of sufficient energy by ACE pigments can render them more responsive to other energy sources, including but not limited to UV and other wavelengths of light. Activated ACE pigments can seemingly also create energy fields, which can be effective in activating other ACE pigments, which can accordingly change from being uncharged, to partially charged and to more fully charged. Direct electrolysis of electrical conductive liquids and/or using Water Gas derived from the electrolysis of electrolyte containing water, can charge both aqueous and oil solutions and enhance their interaction with, and energy transfer to, ACE pigments. Al least for water, charging is associated with an expansion of its molecules, creating a lower density and, presumably, higher energy form. Electrical, electromagnetic and magnetic energies may achieve ACE pathway activation by either charging water or other liquids, with subsequent transfer of the energy to ACE pigments, or by the direct charging of the ACE pigments.

The solubility patterns of neutral red dye and, particularly, the movement patterns of the remaining un-dissolved neutral red particles, have provided a simple method to assess other potential means of charging water, alcohol and other liquids. There are many reports that the consumption of water treated in certain ways can provide significantly greater health benefits than consuming regular water. The benefits have been variously ascribed to an alkaline pH, low oxidative reduction potential (ORP, redox, negative ions), small cluster size or have remained unexplained. Methods have included physical vortexing; exposing water to stationary or rotating magnetic fields, passing water through minerals, including germanium, tourmaline, zeolites and humic acids; inclusion of colloidal minerals, including silver, copper and gold; addition of various herbal products, including terpenes and polyphenols; and even simple sunlight. It is not unreasonable to suggest that clinical efficacy of various waters may correlate with the water's ability to interact with, and transfer energy to, ACE pigments. The neutral red dye linear solubility pattern, along with the neutral red particles movements and interactions, are being assessed as provisional surrogate assessment methods to evaluate various water and other liquid treatment modalities.

The apparent ability of certain charged liquids, including water, to directly interact with ACE pigments, can help explain why even the external application of charged liquids to the skin may have beneficial effects. Current approaches in this endeavor include the use of a simple skin spray to soaking part or all of the body in the treated liquid. Electrolysis units are used in ionic footbaths, which are commonly displayed at health fairs and sold on-line for detoxification. Arguably, the units are producing low density water and water gas, both of which may be entering the feet, or merely interacting with ACE pigments on the skin of the feet. Water gas generated from these units could be used in place of the battery charger and electrolyzer unit, described in the present patent application.

The most immediate applications of the research findings discussed in this patent application, has been the therapeutic use of UV illuminated neutral red solutions. I have switch from using regular alcohol to using charged alcohol with apparent clinical benefit. I can also provide a cost saving by being able to reduce the need for 100% alcohol with the addition of charged water. Sealed plastic bags containing the neutral red solutions can be confidently reused for at least several occasions. Because charging of the alcohol and of the water appears to allow for white light, as well as UV light, to further activate ACE pigments, I can now confidently advocate the use of solutions of charged alcohol diluted into charged water as a beneficial skin spray, even if not followed by directly UV light illumination. At a minimum, these solutions are likely to improve the skin appearance in patients with skin ACE pigments, which can be further stimulated. Since ACE pigments can be shown to circulate in blood (as seen in dark field microscopy), the intravenous injection of osmotically balanced charged water, with or without charged alcohol, would also be expected to enhance systemic ACE activity.

Basically, the newly formulated products will be beneficial for the localized and/or systemic activation of the ACE pathway in patients in whom a deficiency of the ACE pathway is contributing to their illness. Additional information on the ACE pathway and on illnesses, which may benefit from ACE pathway activation, is included in the co-pending patent applications, which are included by reference into this present patent application. The clinical uses of ACE pathway activation can be extended well beyond the treatment of stealth adapted and conventional virus infections. Consideration is being given to activation of the ACE pathway in patients infected with drug resistant bacteria. It should also prove useful as a means of achieving wound healing with minimal scarring from inflammation. Illnesses in which there is an impairment of oxygen delivery to tissues, from metabolic, cardiovascular and/or respiratory causes, can also potentially receive relief from a stimulated ACE pathway. It is, therefore, important to develop methods of simplifying and enhancing the efficiency of ACE pathway activation. This goal has been achieved by the information disclosed in the present patent application.

The principles, preferred embodiments and modes of operation of the present invention have been described in the foregoing specification. The invention, which is intended to be protected herein, is not to be construed as limited to the particular method of charging alcohol and other liquids. I clearly understand now that electrolysis-generated water gas is one of several energy driven processes that may also be able to similarly charge water and other liquids. The use of the term alcohol is also not meant to be restrictive to ethanol, but to also apply to commonly available other alcohols, including methanol and isopropyl alcohol. Similarly, although the patent application refers to neutral red dye, it is known that other dyes, such as acridine orange, can and have been used to activate the ACE pathway. The patent application is, therefore, intended to extend to other dyes and enerceutical products, which can transfer energy to ACE pigments. Additional advantages and modifications of the basic tenets disclosed in the present patent application will readily occur to those skilled in the art and especially upon practicing the currently described methods. Many variations and changes may be made without departing from the scope and spirit of the invention as encompassed by the appended claims. 

1. A method for “charging” a liquid comprising the electrolytic generation of “water gas,” (otherwise known as Brown's Gas or HHO), which is passed through the liquid to be charged, for a sufficient period of time and in a sufficient quantity, for the liquid to show a different type and/or intensity of interaction with particles of added neutral red dye, when this interaction is compared to that seen when a similar amount of neutral red particles is added to the same type of liquid which has not been charged; the most noticeable differences in interaction being i) more rapid dissolving of many of the particles, with linear streams of dissolved neutral red dye coming from individual particles; ii) more rapid and more extensive movements of these particles and of particles which remain un-dissolved, including the continuing to-and-fro movements of some individual particles in relationship to more stationary collections of other particles; the charged liquid plus neutral red dye solution also having an improved capacity, when compared to the same liquid in the uncharged form with a similar amount of neutral red dye, for activating the alternative cellular energy (ACE) pathway of an individual, as shown by the speed of development and/or the intensity of direct UV induced fluorescence of the skin and/or oral cavity, when the charged, compared to the corresponding uncharged, liquid plus neutral red dye solution, is placed onto the skin of ACE deficient individuals and the solutions are similarly illuminated with an ultraviolet (UV) light.
 2. The method of claim 1 in which the liquid to be charged is an alcohol, and in particular, is ethanol.
 3. The method of claim 1, in which the liquid to be charged is water.
 4. The method of claim 1, in which the liquids to be charged include both ethanol and water and which are subsequently used in combination with each other, with added neutral red dye, followed by ultraviolet (UV) light illumination, for the purpose of activating the alternative cellular energy (ACE) pathway of a subject.
 5. The method of claim 1, in which the liquids to be charged include any of the following: herbal formulations, homeopathic formulations, terpenes and/or polyphenol containing solutions, alcoholic beverages; soft drinks; fruit juices; moringa oil; olive oil; cooking oil; and related products.
 6. The method of claim 1, in which the liquids to be charged are intended to direct application to the skin in the form of cosmetics, including skin sprays, shampoos and hair products; footbaths and whole body baths; showers; moistened skin patches; and related products
 7. A means for assessing the effectiveness of a procedure, which is intended to increase the capacity of a liquid to interact with and to provide energy to ACE pigments; the method comprising a determination of whether the procedure is able to modify the type of interaction seen when small numbers of neutral red particles are added to the liquid, such that the procedure is deemed to be effective if there is either i) more rapid dissolving of many of the particles, with longer and more linear streams of dissolved neutral red dye coming from individual particles; ii) more rapid and more extensive movements of these particles and of neutral red particles which remain un-dissolved, including the to-and-fro movements of some individual particles in relationship to more stationary collections of other particles; or iii) more intense fluorescence upon UV illumination of the neutral red containing solution.
 8. The method of claim 7, in which the procedure consists of the passage of “Water Gas,” obtained by electrolysis of water, into the liquid.
 9. The method of claim 7, in which the procedure comprises any of the following: physical vortexing; exposing of the liquid to stationary or rotating magnetic fields; passing water through minerals, including germanium, tourmaline, zeolites and humic acids; inclusion of colloidal minerals, including silver, copper and/or gold; addition of various herbal products, including terpenes and polyphenols; and even simple sunlight. 